[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100655455":3},{"organization":4,"outcomesModule":7,"designInfo":30,"detailedDescription":37,"studyPopulation":29,"armGroups":38,"interventions":51,"overallOfficials":57,"centralContacts":62,"locations":29,"responsibleParty":67,"collaborators":29,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":78,"sex":79,"minAge":80,"maxAge":29,"enrollmentInfo":81,"targetDuration":29,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":92,"whyStopped":29,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":29},{"fullName":5,"class":6},"University of Central Florida","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":29},[9],{"measure":10,"description":11,"timeFrame":12},"Y-Balance Test","Mean Change From Baseline in Y-Balance Test Reach Distance at day 7 . Three recorded trials are completed in the anterior, posteromedial, and posterolateral directions on each limb and averaged.","7 days",[14,17,20,23,26],{"measure":15,"description":16,"timeFrame":12},"Side Hop Test","Change From Baseline in Side Hop Test Score at day 7. Participants perform repeated single-leg side hops across lines 40 centimeters apart for 30 seconds; the highest of two trials is recorded.",{"measure":18,"description":19,"timeFrame":12},"Biodex Balance System","Mean Change From Baseline in Biodex Athlete Single Leg Stability Score at day 7. Three 20-second trials are completed on each lower extremity.",{"measure":21,"description":22,"timeFrame":12},"Grip Strength","Mean Change From Baseline in Handgrip Strength at Day 7. Two maximal contractions are performed with each hand; the highest value for each hand is recorded.",{"measure":24,"description":25,"timeFrame":12},"Tensiomyography","Mean Change From Baseline in Tibialis Anterior Contraction Time at Day 7. Two tensiomyography measurements are obtained for each limb and averaged.",{"measure":27,"description":28,"timeFrame":12},"Confidence Survey","Participant-Reported Comfort, Balance Confidence, Stability, and Willingness to Wear the Assigned Sock at Day 7.",null,{"allocation":31,"interventionModel":32,"interventionModelDescription":33,"primaryPurpose":34,"observationalModel":29,"timePerspective":29,"maskingInfo":35},"RANDOMIZED","PARALLEL","Participants are assigned to one of two sock groups and remain in that group throughout the 7-day intervention period.","TREATMENT",{"masking":36,"maskingDescription":29,"whoMasked":29},"NONE","Participants will attend two in-person visits separated by 7 days. After consent, screening, and baseline testing, participants will be randomized using a computer-generated sequence concealed in sequentially numbered opaque envelopes. Participants will receive either the Trak Ground Wear C001 High-Performance Compression Sock or a commercially available elastic foot and ankle compression sock and will wear it for at least 6 hours per day during waking hours. Assessments include the Y-Balance Test, Side Hop Test, Biodex Balance System, handgrip dynamometry, and tensiomyography of the tibialis anterior. A post-intervention questionnaire will assess perceived comfort, balance confidence, stability, and willingness to wear the assigned sock.",[39,45],{"label":40,"type":41,"description":42,"interventionNames":43},"Novel Tensioning Compression Sock","EXPERIMENTAL","Participants wear the Trak Ground Wear C001 High-Performance Compression Sock during waking hours for at least 6 hours per day for 7 days.",[44],"Other: Novel Tensioning Compression Sock",{"label":46,"type":47,"description":48,"interventionNames":49},"Elastic Compression Sock","ACTIVE_COMPARATOR","Participants wear a commercially available elastic foot and ankle compression sock during waking hours for at least 6 hours per day for 7 days.",[50],"Other: Elastic Compression Sock",[52,55],{"type":6,"name":40,"description":53,"armGroupLabels":54,"otherNames":29},"Participants assigned to the control group will receive a commercially available elastic foot and ankle compression sock. Participants will be instructed to wear their assigned sock during waking hours for a minimum of 6 hours per day over the 7-day intervention period.",[40],{"type":6,"name":46,"description":53,"armGroupLabels":56,"otherNames":29},[46],[58],{"name":59,"affiliation":60,"role":61},"William J Hanney, PhD","UCF","PRINCIPAL_INVESTIGATOR",[63],{"name":59,"role":64,"phone":65,"phoneExt":29,"email":66},"CONTACT","407-823-0217","william.j.hanney@gmail.com",{"type":61,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":29,"oldOrganization":29},"William J. Hanney","Professor","100655455","effects-of-two-compression-socks-on-balance-and-ankle-stability-in-healthy-adults-100655455",false,"NCT07812454","Effects of Two Compression Socks on Balance and Ankle Stability in Healthy Adults","The Effect of a Novel Sock on Ankle Stability, Balance, and Muscle Contraction Time","Not provided","Inclusion Criteria:\n\n* Age 18 years or older\n* Able to perform sit-to-stand, jumping, and single-leg standing without pain or discomfort\n* Able to read, write, and speak sufficient English to complete the study questionnaire\n* Shoe size within the study sock range: men's sizes 4-14 or women's sizes 6-13\n\nExclusion Criteria:\n\n* Feelings of ankle instability\n* An ankle injury within the previous 12 months\n* Previous surgery on either lower extremity\n* History of torn ligaments or cartilage at the hip, knee, or ankle\n* Radicular symptoms in either lower extremity\n* Allergy to sock materials (80 percent nylon, 14 percent polyester, or 6 percent elastane)\n* Unable to consent\n* Pregnant\n* Prisoner",true,"ALL","18 Years",{"count":82,"type":83},52,"ESTIMATED","INTERVENTIONAL",[86],"NA","This randomized study will compare a novel tensioning compression sock with a commercially available elastic foot and ankle compression sock in healthy adults. Participants will wear their assigned sock during waking hours for at least 6 hours per day for 7 days. Balance, ankle stability, grip strength, and tibialis anterior muscle contraction characteristics will be assessed at baseline and after the 7-day intervention. Participants will also report comfort and confidence in balance and stability after the intervention.",[89],"Postural Balance",[91],"Ankle stability; dynamic balance; compression garments; muscle contraction; tensiomyography","NOT_YET_RECRUITING","2026-09-03",{"date":95,"type":96},"2026-09-10","ACTUAL",{"date":98,"type":83},"2026-10-26",{"date":100,"type":83},"2027-10-26",{"name":5,"class":6}]